Xeniolide

Details

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Internal ID c5297b54-20e0-41a2-9dbd-a04cba31ff0c
Taxonomy Organoheterocyclic compounds > Epoxides
IUPAC Name (1S,4Z,9S)-1-methyl-6-methylidene-10-oxabicyclo[7.1.0]dec-4-ene
SMILES (Canonical) CC12CCC=CC(=C)CCC1O2
SMILES (Isomeric) C[C@]12CC/C=C\C(=C)CC[C@@H]1O2
InChI InChI=1S/C11H16O/c1-9-5-3-4-8-11(2)10(12-11)7-6-9/h3,5,10H,1,4,6-8H2,2H3/b5-3-/t10-,11-/m0/s1
InChI Key GVWMTRPEBKLXPR-NBLPHYOQSA-N
Popularity 0 references in papers

Physical and Chemical Properties

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Molecular Formula C11H16O
Molecular Weight 164.24 g/mol
Exact Mass 164.120115130 g/mol
Topological Polar Surface Area (TPSA) 12.50 Ų
XlogP 2.40
Atomic LogP (AlogP) 2.83
H-Bond Acceptor 1
H-Bond Donor 0
Rotatable Bonds 0

Synonyms

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There are no found synonyms.

2D Structure

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2D Structure of Xeniolide

3D Structure

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ADMET Properties (via admetSAR 2)

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Target Value Probability (raw) Probability (%)
Human Intestinal Absorption + 0.9926 99.26%
Caco-2 + 0.8010 80.10%
Blood Brain Barrier + 0.9000 90.00%
Human oral bioavailability + 0.7429 74.29%
Subcellular localzation Lysosomes 0.5323 53.23%
OATP2B1 inhibitior - 0.8535 85.35%
OATP1B1 inhibitior + 0.9534 95.34%
OATP1B3 inhibitior + 0.9558 95.58%
MATE1 inhibitior - 0.9800 98.00%
OCT2 inhibitior - 0.6250 62.50%
BSEP inhibitior - 0.9526 95.26%
P-glycoprotein inhibitior - 0.9849 98.49%
P-glycoprotein substrate - 0.9334 93.34%
CYP3A4 substrate - 0.5000 50.00%
CYP2C9 substrate + 0.5816 58.16%
CYP2D6 substrate - 0.7611 76.11%
CYP3A4 inhibition - 0.8872 88.72%
CYP2C9 inhibition + 0.5812 58.12%
CYP2C19 inhibition + 0.7220 72.20%
CYP2D6 inhibition - 0.9361 93.61%
CYP1A2 inhibition + 0.8624 86.24%
CYP2C8 inhibition - 0.8523 85.23%
CYP inhibitory promiscuity - 0.8257 82.57%
UGT catelyzed - 0.0000 0.00%
Carcinogenicity (binary) - 0.7100 71.00%
Carcinogenicity (trinary) Non-required 0.5056 50.56%
Eye corrosion - 0.8271 82.71%
Eye irritation + 0.7458 74.58%
Skin irritation + 0.5740 57.40%
Skin corrosion - 0.9390 93.90%
Ames mutagenesis - 0.7600 76.00%
Human Ether-a-go-go-Related Gene inhibition - 0.4649 46.49%
Micronuclear - 0.7700 77.00%
Hepatotoxicity + 0.5427 54.27%
skin sensitisation + 0.7672 76.72%
Respiratory toxicity - 0.5222 52.22%
Reproductive toxicity - 0.7991 79.91%
Mitochondrial toxicity - 0.5500 55.00%
Nephrotoxicity - 0.6035 60.35%
Acute Oral Toxicity (c) III 0.7964 79.64%
Estrogen receptor binding - 0.9143 91.43%
Androgen receptor binding - 0.7213 72.13%
Thyroid receptor binding - 0.8421 84.21%
Glucocorticoid receptor binding - 0.7652 76.52%
Aromatase binding - 0.9371 93.71%
PPAR gamma - 0.8132 81.32%
Honey bee toxicity - 0.9397 93.97%
Biodegradation - 0.5000 50.00%
Crustacea aquatic toxicity + 0.5300 53.00%
Fish aquatic toxicity + 0.9207 92.07%

Targets

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Proven Targets:

CHEMBL ID UniProt ID Name Min activity Assay type Source
No proven targets yet!

Predicted Targets (via Super-PRED):

CHEMBL ID UniProt ID Name Probability Model accuracy
CHEMBL5619 P27695 DNA-(apurinic or apyrimidinic site) lyase 90.25% 91.11%
CHEMBL3251 P19838 Nuclear factor NF-kappa-B p105 subunit 88.79% 96.09%
CHEMBL1994 P08235 Mineralocorticoid receptor 86.70% 100.00%
CHEMBL253 P34972 Cannabinoid CB2 receptor 86.03% 97.25%
CHEMBL5608 Q16288 NT-3 growth factor receptor 84.56% 95.89%
CHEMBL230 P35354 Cyclooxygenase-2 84.00% 89.63%
CHEMBL3137262 O60341 LSD1/CoREST complex 83.77% 97.09%
CHEMBL5697 Q9GZT9 Egl nine homolog 1 83.76% 93.40%
CHEMBL4478 Q00975 Voltage-gated N-type calcium channel alpha-1B subunit 80.54% 97.14%
CHEMBL1293249 Q13887 Kruppel-like factor 5 80.34% 86.33%

Plants that contains it

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Below are displayed all the plants proven (via scientific papers) to contain this compound!
To see more specific details click the taxa you are interested in.
Alstonia angustifolia
Alstonia balansae
Alstonia macrophylla

Cross-Links

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PubChem 51350596
LOTUS LTS0257897
wikiData Q105229430